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Some pilot projects have targeted integrating genomics capabilities into providers' electronic health record (EHR) systems as their goal. That project was the first to sequence the genomes of a large group, an endeavor that could benefit population health management. It took Nationwide Children's Hospital in Columbus, Ohio, one week to analyze the same data set that was studied over 18 months during the 1,000 Genomes Project. Strides have been made in genome sequencing efficiency. As technology advances and that data becomes easier to store and comprehend, more healthcare providers will use it to diagnose and treat patients and create clinical decision support. Mapping a human genome is time-consuming and produces a terabyte (TB) of unorganized data. Doing so better enables researchers to understand drug response and disease based on genetics and also helps in the efforts to achieve personalized medicine. When this data is combined with informatics, it enables the integration of all this information. In medicine, next-generation genomic technology can collect increased amounts of genomic data. There are many applications for human genetics in medicine, biotechnology, anthropology and other social sciences. All of that information can be used to form a care plan specific to patients' individual genetic composition, rather than treating them with a one-size-fits-all approach. Genomic studies uncover the genetic makeup of patients, including their genetic differences and mutations. In medicine, genome and DNA sequencing - determining the exact structure of a DNA molecule - are done to learn more about a patient's molecular biology. The human genome typically consists of 23 pairs of chromosomes and 24,000 genes.
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Genomics is the study of human genes and chromosomes. Alex DelVecchio, Content Development Strategist.
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